Canonical Allele Identifier: CA16031712

Gene: APC

Linked Data

• dbSNP Id: rs2149922368
• MyVariant Identifiers: chr5:g.112176024G>A (hg19) ; chr5:g.112840327G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840327G>A , CM000667.2:g.112840327G>A	GRCh38
NC_000005.9:g.112176024G>A , CM000667.1:g.112176024G>A	GRCh37
NC_000005.8:g.112203923G>A	NCBI36
NG_008481.4:g.152807G>A , LRG_130:g.152807G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4787G>A	ENSP00000473355.2:p.Cys1596Tyr
ENST00000505350.2:c.*4739G>A	ENSP00000481752.1:n.*4739G>A
ENST00000507379.6:c.4679G>A	ENSP00000423224.2:p.Cys1560Tyr
ENST00000509732.6:c.4733G>A	ENSP00000426541.2:p.Cys1578Tyr
ENST00000512211.7:c.4733G>A	ENSP00000423828.3:p.Cys1578Tyr
ENST00000257430.9:c.4733G>A MANE Select	ENSP00000257430.4:p.Cys1578Tyr
ENST00000257430.8:c.4733G>A	ENSP00000257430.4:p.Cys1578Tyr
ENST00000508376.6:c.4733G>A	ENSP00000427089.2:p.Cys1578Tyr
ENST00000508624.5:c.*4055G>A	ENSP00000424265.1:n.*4055G>A
ENST00000520401.1:c.230+11355G>A
NM_000038.5:c.4733G>A	NP_000029.2:p.Cys1578Tyr
NM_001127510.2:c.4733G>A	NP_001120982.1:p.Cys1578Tyr
NM_001127511.2:c.4679G>A	NP_001120983.2:p.Cys1560Tyr
NM_001354895.1:c.4733G>A	NP_001341824.1:p.Cys1578Tyr
NM_001354896.1:c.4787G>A	NP_001341825.1:p.Cys1596Tyr
NM_001354897.1:c.4763G>A	NP_001341826.1:p.Cys1588Tyr
NM_001354898.1:c.4658G>A	NP_001341827.1:p.Cys1553Tyr
NM_001354899.1:c.4649G>A	NP_001341828.1:p.Cys1550Tyr
NM_001354900.1:c.4610G>A	NP_001341829.1:p.Cys1537Tyr
NM_001354901.1:c.4556G>A	NP_001341830.1:p.Cys1519Tyr
NM_001354902.1:c.4460G>A	NP_001341831.1:p.Cys1487Tyr
NM_001354903.1:c.4430G>A	NP_001341832.1:p.Cys1477Tyr
NM_001354904.1:c.4355G>A	NP_001341833.1:p.Cys1452Tyr
NM_001354905.1:c.4253G>A	NP_001341834.1:p.Cys1418Tyr
NM_001354906.1:c.3884G>A	NP_001341835.1:p.Cys1295Tyr
NM_000038.6:c.4733G>A MANE Select	NP_000029.2:p.Cys1578Tyr
NM_001127510.3:c.4733G>A	NP_001120982.1:p.Cys1578Tyr
NM_001127511.3:c.4679G>A	NP_001120983.2:p.Cys1560Tyr
NM_001354895.2:c.4733G>A	NP_001341824.1:p.Cys1578Tyr
NM_001354896.2:c.4787G>A	NP_001341825.1:p.Cys1596Tyr
NM_001354897.2:c.4763G>A	NP_001341826.1:p.Cys1588Tyr
NM_001354898.2:c.4658G>A	NP_001341827.1:p.Cys1553Tyr
NM_001354899.2:c.4649G>A	NP_001341828.1:p.Cys1550Tyr
NM_001354900.2:c.4610G>A	NP_001341829.1:p.Cys1537Tyr
NM_001354901.2:c.4556G>A	NP_001341830.1:p.Cys1519Tyr
NM_001354902.2:c.4460G>A	NP_001341831.1:p.Cys1487Tyr
NM_001354903.2:c.4430G>A	NP_001341832.1:p.Cys1477Tyr
NM_001354904.2:c.4355G>A	NP_001341833.1:p.Cys1452Tyr
NM_001354905.2:c.4253G>A	NP_001341834.1:p.Cys1418Tyr
NM_001354906.2:c.3884G>A	NP_001341835.1:p.Cys1295Tyr